A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1276n100



Internal ID20152892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107693548..108059223hg38UCSC Ensembl
chr11:107564274..107929950hg19UCSC Ensembl
chr11:107069484..107435160hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38365676
hg19365677
hg18365677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038581, nsv1048938
Samples
Known GenesCUL5, RAB39A, SLC35F2, SLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1276n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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